Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)
Location

Chromosome 13:27920235 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM056344

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB IPF1_97C_A_051911

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts, has 2504 individual genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variation displays